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    Results: 1 to 20 of 310

    1.

    Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis.

    Gaitanou M, Buanne P, Pappa C, Georgopoulou N, Mamalaki A, Tirone F, Matsas R.

    Biochem J. 2001 May 1;355(Pt 3):715-24.PMID: 11311134 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5.

    Zhu X, Higashimoto K, Soejima H, Yatsuki H, Sugihara H, Mukai T, Joh K.

    Gene. 2000 Oct 3;256(1-2):311-7.PMID: 11054561 [PubMed - indexed for MEDLINE]Related articles

    3.

    Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer.

    Lorenzi MV, Castagnino P, Aaronson DC, Lieb DC, Lee CC, Keck CL, Popescu NC, Miki T.

    Genomics. 1999 Nov 15;62(1):59-66.PMID: 10585768 [PubMed - indexed for MEDLINE]Related articles

    4.

    Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.

    Cooper PR, Smilinich NJ, Day CD, Nowak NJ, Reid LH, Pearsall RS, Reece M, Prawitt D, Landers J, Housman DE, Winterpacht A, Zabel BU, Pelletier J, Weissman BE, Shows TB, Higgins MJ.

    Genomics. 1998 Apr 1;49(1):38-51.PMID: 9570947 [PubMed - indexed for MEDLINE]Related articles

    5.

    Molecular cloning and in situ localization of the human contactin gene (CNTN1) on chromosome 12q11-q12.

    Berglund EO, Ranscht B.

    Genomics. 1994 Jun;21(3):571-82.PMID: 7959734 [PubMed - indexed for MEDLINE]Related articles

    6.

    JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.

    Morita R, Miyazaki E, Fong CY, Chen XN, Korenberg JR, Delgado-Escueta AV, Yamakawa K.

    Biochem Biophys Res Commun. 1998 Jul 20;248(2):307-14. Erratum in: Biochem Biophys Res Commun 1998 Sep 18;250(2):536. PMID: 9675132 [PubMed - indexed for MEDLINE]Related articles

    7.

    Expression pattern of BM88 in the developing nervous system of the chick and mouse embryo.

    Politis PK, Rohrer H, Matsas R.

    Gene Expr Patterns. 2007 Jan;7(1-2):165-77. Epub 2006 Jul 4.PMID: 16949349 [PubMed - indexed for MEDLINE]Related articles

    8.

    cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 protein.

    Bressler SL, Gray MD, Sopher BL, Hu Q, Hearn MG, Pham DG, Dinulos MB, Fukuchi K, Sisodia SS, Miller MA, Disteche CM, Martin GM.

    Hum Mol Genet. 1996 Oct;5(10):1589-98.PMID: 8894693 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

    Paulsen M, Davies KR, Bowden LM, Villar AJ, Franck O, Fuermann M, Dean WL, Moore TF, Rodrigues N, Davies KE, Hu RJ, Feinberg AP, Maher ER, Reik W, Walter J.

    Hum Mol Genet. 1998 Jul;7(7):1149-59.PMID: 9618174 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Identification and chromosome mapping of the mouse homologue of the human gene (DDX6) that encodes a putative RNA helicase of the DEAD box protein family.

    Akao Y, Matsuda Y.

    Cytogenet Cell Genet. 1996;75(1):38-44.PMID: 8995487 [PubMed - indexed for MEDLINE]Related articles

    11.

    Cloning of the human interferon-related developmental regulator (IFRD1) gene coding for the PC4 protein, a member of a novel family of developmentally regulated genes.

    Buanne P, Incerti B, Guardavaccaro D, Avvantaggiato V, Simeone A, Tirone F.

    Genomics. 1998 Jul 15;51(2):233-42.PMID: 9722946 [PubMed - indexed for MEDLINE]Related articles

    12.

    Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.

    Yatsuki H, Watanabe H, Hattori M, Joh K, Soejima H, Komoda H, Xin Z, Zhu X, Higashimoto K, Nishimura M, Kuratomi S, Sasaki H, Sakaki Y, Mukai T.

    DNA Res. 2000 Jun 30;7(3):195-206.PMID: 10907850 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes]

    Zhang DL, Ji L, Li YD.

    Yi Chuan Xue Bao. 2004 May;31(5):431-43. Chinese. PMID: 15478601 [PubMed - indexed for MEDLINE]Related articles

    14.

    11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.

    Puech A, Ahnine L, Lüdecke HJ, Senger G, Ivens A, Jeanpierre C, Little P, Horsthemke B, Claussen U, Jones C, et al.

    Genomics. 1992 Aug;13(4):1274-80.PMID: 1380484 [PubMed - indexed for MEDLINE]Related articles

    15.

    Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.

    Boultwood J, Fidler C, Strickson AJ, Watkins F, Kostrzewa M, Jaju RJ, Müller U, Wainscoat JS.

    Genomics. 2000 May 15;66(1):26-34.PMID: 10843801 [PubMed - indexed for MEDLINE]Related articles

    16.

    Cloning, mapping, and tissue distribution of a human homologue of the mouse jerky gene product.

    Zeng Z, Kyaw H, Gakenheimer KR, Augustus M, Fan P, Zhang X, Su K, Carter KC, Li Y.

    Biochem Biophys Res Commun. 1997 Jul 18;236(2):389-95.PMID: 9240447 [PubMed - indexed for MEDLINE]Related articles

    17.

    Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression.

    Prawitt D, Enklaar T, Klemm G, Gärtner B, Spangenberg C, Winterpacht A, Higgins M, Pelletier J, Zabel B.

    Hum Mol Genet. 2000 Jan 22;9(2):203-16.PMID: 10607831 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Alternative splicing, chromosome assignment and subcellular localization of the testicular haploid expressed gene (THEG).

    Mannan A, Lücke K, Dixkens C, Neesen J, Kämper M, Engel W, Burfeind P.

    Cytogenet Cell Genet. 2000;91(1-4):171-9.PMID: 11173852 [PubMed - indexed for MEDLINE]Related articles

    19.

    The human reelin gene: isolation, sequencing, and mapping on chromosome 7.

    DeSilva U, D'Arcangelo G, Braden VV, Chen J, Miao GG, Curran T, Green ED.

    Genome Res. 1997 Feb;7(2):157-64.PMID: 9049633 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    The BM88 antigen, a novel neuron-specific molecule, enhances the differentiation of mouse neuroblastoma cells.

    Mamalaki A, Boutou E, Hurel C, Patsavoudi E, Tzartos S, Matsas R.

    J Biol Chem. 1995 Jun 9;270(23):14201-8.PMID: 7775480 [PubMed - indexed for MEDLINE]Related articlesFree article

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